Acid Reducer
- Product NDC
- 37808-876
- 11-digit product format
- 378080876
- Labeler code
- 37808
- Product ID
- 37808-876_f1ee4481-93bb-4637-8b25-510a32a97c19
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA076195
- Marketing category
- ANDA
- Marketing start
- 2016-10-27
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 37808-876-47 | 37808087647 | 1 BOTTLE in 1 CARTON (37808-876-47) > 150 TABLET, COATED in 1 BOTTLE | 1 bottle | 2016-10-27 | 0000-00-00 | No | No | Current |
| 37808-876-65 | 37808087665 | 1 BOTTLE in 1 CARTON (37808-876-65) > 30 TABLET, COATED in 1 BOTTLE | 1 bottle | 2016-10-27 | 0000-00-00 | No | No | Current |